Zimmer Biomet recalls Coonrad/Morrey Total Elbow Humeral Assembly model 32-8105-027-04 due to two outer pins instead of one inner and one outer pin, which may cause improper joint function.
The lot contained two outer pins instead of one outer and one inner pin.
Zimmer Biomet is recalling a specific elbow prosthesis model because it contains two outer pins instead of one inner and one outer pin. This defect could lead to improper joint function and potential complications after surgery.
The prosthesis has two outer pins instead of one inner and one outer pin. This design flaw may cause improper joint alignment and function after surgery, potentially leading to complications.
Patients who received the recalled model 32-8105-027-04 elbow prosthesis during surgery are affected. Surgeons and medical staff who used this model are at highest risk for improper implant function.
Check for the model number 32-8105-027-04 on the prosthesis. The recall covers lot number 64481139.
Verify the model number on the prosthesis is 32-8105-027-04.
The recall is for a design defect that may cause improper joint function, but it does not indicate an immediate risk of serious injury.
Check the model number on the prosthesis; the recalled model is 32-8105-027-04 with lot number 64481139.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1000-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1000-2020 from Zimmer Biomet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
